Job Details

Work Shift:
DAY

Work Schedule:

Why Merit?

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.

ESSENTIAL FUNCTIONS PERFORMED

1. Sets up and maintains trial master file and is responsible for filing and maintaining up to date study documents.

2. Maintains multiple trackers following the progress of assigned clinical trials, such as essential documents, investigational product, trial supplies and study follow-up visits, as applicable.

3. Orders, prepares, and sends documents and materials to clinical trial sites and vendors as needed (electronic and paper).

4. Provides support to study vendors.

5. Collects and reviews all regulatory documents for accuracy and compliance to departmental SOPs, local and national regulations and guidelines. Follows up as required to resolve deficiencies.

6. Ensures that regulatory documents are maintained and updated in a timely and appropriate manner.

7. Ensures study team training records are kept current.

8. Performs in-house duties to assist monitors, e.g., outstanding action items.

9. Manages central IRB submissions and supports sites in IRB/EC submissions.

10. May attend site visits to assist monitors, when applicable.

11. Assists with the development of study and site tools.

12. Contribute to clinical site interactions, including enrollment and subject visit updates, clinical trial material and clinical supply requests, issue resolution, etc.

13. Assist in developing and overseeing study operational plan(s) as applicable (e.g., TMF plan).

14. Contribute to study team for trial start-up, conduct, and close-out activities according to industry and departmental standards.

15. Conduct study systems training(s).

16. Contribute to creation of study documentation including informed consent, newsletters, etc.

17. Provides general support to the Clinical Affairs team and project team(s), including meeting agendas, minutes and management of translations.

18. Assist Project Managers with invoice receipt and review as applicable.

19. Perform other duties and tasks, as required.

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS

• Lifting -- Not to exceed 50 lbs. - local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Visual acuity
• Color perception
• Depth perception
• Reading
• Field of vision/peripheral

SUMMARY OF MINIMUM QUALIFICATIONS

• Education and/or experience equivalent to a Bachelor's Degree in a scientific discipline or nursing qualification.

• A minimum of six (6) years of related work experience.

• Current Good Clinical Practice (GCP) certification

• Knowledge of US regulations, Good Clinical Practice and ICH guidelines.

• Demonstrated computer skills preferably spreadsheets, word processing, database and other applicable software programs.

• Clinical trial experience.

PREFERRED QUALIFICATIONS

• Medical Device clinical trial experience

COMPETENCIES

• Verbal and written communication
• Organization
• Detail-oriented
• Project task team participation

COMMENTS

Infectious Control Risk Category III:

The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category III states employment and procedures that do not require exposure.

As an eligible Merit employee, you can expect the following:

* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights

* Medical/Dental & Other Insurances (eligible the first of month after 30 days)

* Low Cost Onsite Medical Clinic

* Two (2) Onsite Cafeterias

* Employee Garden | Gardening Classes

* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays

* 401K | Health Savings Account

To see more on our culture, go to www.merit.com/careers.

Military Veterans are encouraged to Apply.

Merit is a proud Utah Patriot Partner committed to hiring our Veterans.